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"Osti" extracorporeal shock wave lithotripter - Taiwan Registration 09651c659a99cf7106913584d828c7fb

Access comprehensive regulatory information for "Osti" extracorporeal shock wave lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09651c659a99cf7106913584d828c7fb and manufactured by AST GMBH. The authorized representative in Taiwan is LITHO MED TRADING CO., LTD..

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09651c659a99cf7106913584d828c7fb
Registration Details
Taiwan FDA Registration: 09651c659a99cf7106913584d828c7fb
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Device Details

"Osti" extracorporeal shock wave lithotripter
TW: โ€œๅฅงๆ–ฏๅ คโ€้ซ”ๅค–้œ‡ๆณข็ขŽ็ŸณๆฉŸ
Risk Class 2
Cancelled

Registration Details

09651c659a99cf7106913584d828c7fb

DHA00602056102

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.5990 ้ซ”ๅค–้œ‡ๆณข็ขŽ็Ÿณๅ™จ

The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input

Dates and Status

Jan 26, 2010

Jan 26, 2015

Aug 14, 2018

Cancellation Information

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